A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1030821



Internal ID19120040
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:5065723..5081941hg38UCSC Ensembl
Innerchr9:5065723..5081941hg19UCSC Ensembl
Innerchr9:5055723..5071941hg18UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg3816219
hg1916219
hg1816219
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7383n100
Supporting Variantsnssv3692405
Samples
Known GenesJAK2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1030821
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer